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Prion|August 17, 2011
Genome wide association studies and prion diseaseAna Lukic, Simon Mead
Acta Neuropathologica Communications|November 21, 2013
Filamentous white matter prion protein deposition is a distinctive feature of multiple inherited prion diseasesLilla Reiniger, Ilaria Mirabile, Ana Lukic, et al.
Neurobiology of Disease|June 23, 2020
Genetic risk factors for Creutzfeldt-Jakob diseaseEmma Jones, Simon Mead
Dementia and Geriatric Cognitive Disorders Extra|September 11, 2012
Video Rating in Neurodegenerative Disease Clinical Trials: The Experience of PRION-1Christopher Carswell, Michael Rañopa, Suvankar Pal, et al.
Science (New York, N.Y.)|November 10, 2007
A general model of prion strains and their pathogenicityJohn Collinge, Anthony R Clarke
Trends in Microbiology|December 9, 2003
Subclinical prion infectionAndrew F Hill, John Collinge
APMIS : Acta Pathologica, Microbiologica, Et Immunologica Scandinavica|June 18, 2002
Species-barrier-independent prion replication in apparently resistant speciesAndrew F Hill, John Collinge
British Medical Bulletin|October 3, 2003
Subclinical prion infection in humans and animalsAndrew F Hill, John Collinge
Brain : a Journal of Neurology|July 4, 2006
A systematic review of prion therapeutics in experimental modelsClare R Trevitt, John Collinge
Infectious Disorders Drug Targets|February 10, 2009
Preventing prion pathogenicity by targeting the cellular prion proteinAndrew J Nicoll, John Collinge
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